4.6 Article

Sex-Specific Reproductive Factors Augment Cardiovascular Disease Risk in Women: A Mendelian Randomization Study

Journal

Publisher

WILEY
DOI: 10.1161/JAHA.122.027933

Keywords

age at first birth; cardiovascular disease; menarche; menopause; parity; reproductive

Ask authors/readers for more resources

This study used Mendelian randomization to explore the causal relevance of reproductive factors on cardiovascular disease in women. The results showed that earlier genetically predicted age at first birth, higher genetically predicted number of live births, and earlier genetically predicted age at menarche were associated with increased risk of cardiovascular disease. These findings support the role of reproductive factors in the development of cardiovascular disease in women and identify potential modifiable mediators for clinical intervention.
BackgroundObservational studies suggest that reproductive factors are associated with cardiovascular disease, but these are liable to influence by residual confounding. This study explores the causal relevance of reproductive factors on cardiovascular disease in women using Mendelian randomization. Methods and ResultsUncorrelated (r(2)<0.001), genome-wide significant (P<5x10(-8)) single-nucleotide polymorphisms were extracted from sex-specific genome-wide association studies of age at first birth, number of live births, age at menarche, and age at menopause. Inverse-variance weighted Mendelian randomization was used for primary analyses on outcomes of atrial fibrillation, coronary artery disease, heart failure, ischemic stroke, and stroke. Earlier genetically predicted age at first birth increased risk of coronary artery disease (odds ratio [OR] per year, 1.49 [95% CI, 1.28-1.74], P=3.72x10(-7)) heart failure (OR, 1.27 [95% CI, 1.06-1.53], P=0.009), and stroke (OR, 1.25 [95% CI, 1.00-1.56], P=0.048), with partial mediation through body mass index, type 2 diabetes, blood pressure, and cholesterol traits. Higher genetically predicted number of live births increased risk of atrial fibrillation (OR for <2, versus 2, versus >2 live births, 2.91 [95% CI, 1.16-7.29], P=0.023), heart failure (OR, 1.90 [95% CI, 1.28-2.82], P=0.001), ischemic stroke (OR, 1.86 [95% CI, 1.03-3.37], P=0.039), and stroke (OR, 2.07 [95% CI, 1.22-3.52], P=0.007). Earlier genetically predicted age at menarche increased risk of coronary artery disease (OR per year, 1.10 [95% CI, 1.06-1.14], P=1.68x10(-6)) and heart failure (OR, 1.12 [95% CI, 1.07-1.17], P=5.06x10(-7)); both associations were at least partly mediated by body mass index. ConclusionsThese results support a causal role of a number of reproductive factors on cardiovascular disease in women and identify multiple modifiable mediators amenable to clinical intervention.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available